Cargando…

Nectary development in Cleome violacea

Nectaries are a promising frontier for plant evo-devo research, and are particularly fascinating given their diversity in form, position, and secretion methods across angiosperms. Emerging model systems permit investigations of the molecular basis for nectary development and nectar secretion across...

Descripción completa

Detalles Bibliográficos
Autores principales: Carey, Shane, Zenchyzen, Brandi, Deneka, A. J., Hall, Jocelyn C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949531/
https://www.ncbi.nlm.nih.gov/pubmed/36844906
http://dx.doi.org/10.3389/fpls.2022.1085900
_version_ 1784892972216614912
author Carey, Shane
Zenchyzen, Brandi
Deneka, A. J.
Hall, Jocelyn C.
author_facet Carey, Shane
Zenchyzen, Brandi
Deneka, A. J.
Hall, Jocelyn C.
author_sort Carey, Shane
collection PubMed
description Nectaries are a promising frontier for plant evo-devo research, and are particularly fascinating given their diversity in form, position, and secretion methods across angiosperms. Emerging model systems permit investigations of the molecular basis for nectary development and nectar secretion across a range of taxa, which addresses fundamental questions about underlying parallelisms and convergence. Herein, we explore nectary development and nectar secretion in the emerging model taxa, Cleome violacea (Cleomaceae), which exhibits a prominent adaxial nectary. First, we characterized nectary anatomy and quantified nectar secretion to establish a foundation for quantitative and functional gene experiments. Next, we leveraged RNA-seq to establish gene expression profiles of nectaries across three key stages of development: pre-anthesis, anthesis, and post-fertilization. We then performed functional studies on five genes that were putatively involved in nectary and nectar formation: CvCRABSCLAW (CvCRC), CvAGAMOUS (CvAG), CvSHATTERPROOF (CvSHP), CvSWEET9, and a highly expressed but uncharacterized transcript. These experiments revealed a high degree of functional convergence to homologues from other core Eudicots, especially Arabidopsis. CvCRC, redundantly with CvAG and CvSHP, are required for nectary initiation. Concordantly, CvSWEET9 is essential for nectar formation and secretion, which indicates that the process is eccrine based in C. violacea. While demonstration of conservation is informative to our understanding of nectary evolution, questions remain. For example, it is unknown which genes are downstream of the developmental initiators CvCRC, CvAG, and CvSHP, or what role the TCP gene family plays in nectary initiation in this family. Further to this, we have initiated a characterization of associations between nectaries, yeast, and bacteria, but more research is required beyond establishing their presence. Cleome violacea is an excellent model for continued research into nectary development because of its conspicuous nectaries, short generation time, and close taxonomic distance to Arabidopsis.
format Online
Article
Text
id pubmed-9949531
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-99495312023-02-24 Nectary development in Cleome violacea Carey, Shane Zenchyzen, Brandi Deneka, A. J. Hall, Jocelyn C. Front Plant Sci Plant Science Nectaries are a promising frontier for plant evo-devo research, and are particularly fascinating given their diversity in form, position, and secretion methods across angiosperms. Emerging model systems permit investigations of the molecular basis for nectary development and nectar secretion across a range of taxa, which addresses fundamental questions about underlying parallelisms and convergence. Herein, we explore nectary development and nectar secretion in the emerging model taxa, Cleome violacea (Cleomaceae), which exhibits a prominent adaxial nectary. First, we characterized nectary anatomy and quantified nectar secretion to establish a foundation for quantitative and functional gene experiments. Next, we leveraged RNA-seq to establish gene expression profiles of nectaries across three key stages of development: pre-anthesis, anthesis, and post-fertilization. We then performed functional studies on five genes that were putatively involved in nectary and nectar formation: CvCRABSCLAW (CvCRC), CvAGAMOUS (CvAG), CvSHATTERPROOF (CvSHP), CvSWEET9, and a highly expressed but uncharacterized transcript. These experiments revealed a high degree of functional convergence to homologues from other core Eudicots, especially Arabidopsis. CvCRC, redundantly with CvAG and CvSHP, are required for nectary initiation. Concordantly, CvSWEET9 is essential for nectar formation and secretion, which indicates that the process is eccrine based in C. violacea. While demonstration of conservation is informative to our understanding of nectary evolution, questions remain. For example, it is unknown which genes are downstream of the developmental initiators CvCRC, CvAG, and CvSHP, or what role the TCP gene family plays in nectary initiation in this family. Further to this, we have initiated a characterization of associations between nectaries, yeast, and bacteria, but more research is required beyond establishing their presence. Cleome violacea is an excellent model for continued research into nectary development because of its conspicuous nectaries, short generation time, and close taxonomic distance to Arabidopsis. Frontiers Media S.A. 2023-02-09 /pmc/articles/PMC9949531/ /pubmed/36844906 http://dx.doi.org/10.3389/fpls.2022.1085900 Text en Copyright © 2023 Carey, Zenchyzen, Deneka and Hall https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Carey, Shane
Zenchyzen, Brandi
Deneka, A. J.
Hall, Jocelyn C.
Nectary development in Cleome violacea
title Nectary development in Cleome violacea
title_full Nectary development in Cleome violacea
title_fullStr Nectary development in Cleome violacea
title_full_unstemmed Nectary development in Cleome violacea
title_short Nectary development in Cleome violacea
title_sort nectary development in cleome violacea
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9949531/
https://www.ncbi.nlm.nih.gov/pubmed/36844906
http://dx.doi.org/10.3389/fpls.2022.1085900
work_keys_str_mv AT careyshane nectarydevelopmentincleomeviolacea
AT zenchyzenbrandi nectarydevelopmentincleomeviolacea
AT denekaaj nectarydevelopmentincleomeviolacea
AT halljocelync nectarydevelopmentincleomeviolacea